Tarragó David, Casal Julio, Ruiz-Contreras Jesús, Ramos J Tomás, Rojo Pablo, Snippe Harm, Jansen Wouter T M
Department of Bacteriology, National Center for Microbiology, Lab. C-11, Instituto de Salud Carlos III, Carretera Majadahonda-Pozuelo km 2, 28220 Majadahonda, Madrid, Spain.
Clin Diagn Lab Immunol. 2005 Jan;12(1):165-70. doi: 10.1128/CDLI.12.1.165-170.2005.
We investigated antibody responses against pneumococci of serotypes 6B, 14, and 23F in 56 children and adolescents with perinatal human immunodeficiency virus (HIV) infection who were vaccinated with 7-valent pneumococcal conjugate vaccine. Overall immune responses differed greatly between serotypes. Correlation coefficients between immunoglobulin G (IgG) measured by enzyme-linked immunosorbent assay (ELISA) and functional antibodies measured by a flow cytometry opsonophagocytosis assay (OPA) varied with serotype and time points studied. After 3 months of administering a second PCV7 dose we got the highest correlation (with significant r values of 0.754, 0.414, and 0.593 for serotypes 6B, 14, and 23F, respectively) but no significant increase in IgG concentration and OPA titers compared to the first dose. We defined a responder to a serotype included in the vaccine with two criteria: frequency of at least twofold OPA and ELISA increases for each serotype and frequency of conversion from negative to positive OPA levels. Responders varied from 43.9% to 46.3%, 28.5% to 50.0%, and 38.0% to 50.0% for serotypes 6B, 14, and 23F, respectively, depending on the response criterion. The present research highlights the importance of demonstrating vaccine immunogenicity with suitable immunological endpoints in immunocompromised patients and also the need to define how much antibody is required for protection from different serotypes, since immunogenicity differed significantly between serotypes.
我们调查了56名围产期感染人类免疫缺陷病毒(HIV)的儿童和青少年接种7价肺炎球菌结合疫苗后针对6B、14和23F血清型肺炎球菌的抗体反应。各血清型的总体免疫反应差异很大。通过酶联免疫吸附测定(ELISA)测得的免疫球蛋白G(IgG)与通过流式细胞术调理吞噬测定(OPA)测得的功能性抗体之间的相关系数随所研究的血清型和时间点而变化。在接种第二剂PCV7三个月后,我们得到了最高的相关性(6B、14和23F血清型的r值分别为0.754、0.414和0.593,均具有显著性),但与第一剂相比,IgG浓度和OPA滴度没有显著增加。我们用两个标准来定义对疫苗中包含的血清型有反应者:每种血清型的OPA和ELISA至少增加两倍的频率以及OPA水平从阴性转为阳性的频率。根据反应标准,6B、14和23F血清型的有反应者分别为43.9%至46.3%、28.5%至50.0%和38.0%至50.0%。本研究强调了在免疫功能低下的患者中用合适的免疫终点来证明疫苗免疫原性的重要性,也强调了需要确定针对不同血清型的保护所需的抗体量,因为各血清型的免疫原性差异显著。